Vissers M C, Wiggins R, Fantone J C
Department of Pathology, University of Michigan Medical School, Ann Arbor.
Lab Invest. 1989 Jun;60(6):831-8.
We have compared the ability of human peripheral blood monocytes and neutrophils to degrade glomerular basement membrane (GBM) in vitro. When isolated cells were incubated with GBM containing anti-GBM immune complexes, both neutrophils and monocytes adhered and spread on the surface of the GBM, underwent a respiratory burst and released lysosomal enzymes into the medium. With neutrophils, this resulted in rapid degradation of the GBM, measured both as solubilization of collagenous and noncollagenous protein. In contrast, monocytes degraded GBM very slowly, with a slight increase in the rate of hydroxyproline solubilization after approximately 24 hours incubation. Degradation of GBM by neutrophils was predominantly due to the action of serine proteinases, whereas inhibition of monocyte-mediated hydroxyproline release required both phenylmethylsulfonyl fluoride and o-phenanthroline, suggesting some synergy between serine and metalloproteinases. The results indicate that neutrophils are more able to degrade GBM components than are monocytes, and suggest that they may be capable of greater damage to the GBM in vivo, mostly due to their higher proteolytic capacity.
我们比较了人外周血单核细胞和中性粒细胞在体外降解肾小球基底膜(GBM)的能力。当将分离出的细胞与含有抗GBM免疫复合物的GBM一起孵育时,中性粒细胞和单核细胞均会黏附并铺展在GBM表面,发生呼吸爆发,并将溶酶体酶释放到培养基中。对于中性粒细胞,这导致GBM迅速降解,这可通过胶原和非胶原蛋白质的溶解来衡量。相比之下,单核细胞降解GBM非常缓慢,在孵育约24小时后羟脯氨酸溶解速率略有增加。中性粒细胞对GBM的降解主要归因于丝氨酸蛋白酶的作用,而抑制单核细胞介导的羟脯氨酸释放则需要苯甲基磺酰氟和邻菲罗啉,这表明丝氨酸蛋白酶和金属蛋白酶之间存在某种协同作用。结果表明,中性粒细胞比单核细胞更能降解GBM成分,这表明它们在体内可能对GBM造成更大的损害,这主要是由于它们具有更高的蛋白水解能力。